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rs375330016

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375330016(A;A)
Make rs375330016(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position70176084
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs375330016
ebirs375330016
HLIrs375330016
Exacrs375330016
Varsomers375330016
Maprs375330016
PheGenIrs375330016
hapmaprs375330016
1000 genomesrs375330016
hgdprs375330016
ensemblrs375330016
gopubmedrs375330016
geneviewrs375330016
scholarrs375330016
googlers375330016
pharmgkbrs375330016
gwascentralrs375330016
openSNPrs375330016
23andMers375330016
23andMe allrs375330016
SNP Nexus

SNPshotrs375330016
SNPdbers375330016
MSV3drs375330016
GWAS Ctlgrs375330016
Max Magnitude0
ClinVar
Risk rs375330016(A;A)
Alt rs375330016(A;A)
Reference rs375330016(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNJ2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.68172225G>A
CLNSRC
CLNACC RCV000170990.2,